ReP USP - Resultado da busca

Artigo de periodico
Copper-catalyzed NeH insertion reactions from sulfoxonium ylides (2020)
Furniel, Lucas Giani; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Subjects: CATÁLISE, COBRE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FURNIEL, Lucas Giani e BURTOLOSO, Antonio Carlos Bender. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, v. 76, n. 51, p. 131313, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2020.131313. Acesso em: 03 nov. 2024.
APA
Furniel, L. G., & Burtoloso, A. C. B. (2020). Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, 76( 51), 131313. doi:10.1016/j.tet.2020.131313
NLM
Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ; 76( 51): 131313.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2020.131313
Vancouver
Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ; 76( 51): 131313.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2020.131313
Artigo de periodico
Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry (2020)
Perecim, Givago P.; Deflon, Victor Marcelo ; Martins, Gabriel R.; Pinto, Leandro M.C.; Casagrande, Gleison Antônio ; Silva, Diogo Oliveira; Raminelli, Cristiano
Source: Tetrahedron. Unidade: IQSC
Subjects: ALCALOIDES, QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERECIM, Givago P. et al. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, v. 76. 131461 July 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2020.131461. Acesso em: 03 nov. 2024.
APA
Perecim, G. P., Deflon, V. M., Martins, G. R., Pinto, L. M. C., Casagrande, G. A., Silva, D. O., & Raminelli, C. (2020). Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, 76. 131461 July 2020. doi:10.1016/j.tet.2020.131461
NLM
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2020.131461
Vancouver
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2020.131461
Artigo de periodico
One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin (2017)
Dias, Rafael Mafra de Paula; Momo, Patrícia Betoni; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Rafael Mafra de Paula e MOMO, Patrícia Betoni e BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, v. 73, n. 26, p. 3720 - 3729, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2017.05.040. Acesso em: 03 nov. 2024.
APA
Dias, R. M. de P., Momo, P. B., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, 73( 26), 3720 - 3729. doi:10.1016/j.tet.2017.05.040
NLM
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Vancouver
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Artigo de periodico
Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol (2017)
Lima, Rafaely Nascimento; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Assunto: QUÍMICA VERDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Rafaely Nascimento e PORTO, Andre Luiz Meleiro. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, v. 58, n. 9, p. 825-828, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.12.062. Acesso em: 03 nov. 2024.
APA
Lima, R. N., & Porto, A. L. M. (2017). Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, 58( 9), 825-828. doi:10.1016/j.tetlet.2016.12.062
NLM
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Vancouver
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Artigo de periodico
Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 (2016)
Jimenez, David Esteban Quintero; Ferreira , Irlon Maciel; Birolli, Willian Garcia; Fonseca, Luis P.; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Subjects: FUNGOS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JIMENEZ, David Esteban Quintero et al. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, v. 72, n. 46, p. 7317-7322, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2016.02.014. Acesso em: 03 nov. 2024.
APA
Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
NLM
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Vancouver
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Artigo de periodico
A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal (2014)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, v. 70, p. 3291-3296, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.10.059. Acesso em: 03 nov. 2024.
APA
Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
NLM
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Vancouver
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Artigo de periodico
Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones (2008)
Burtoloso, Antonio Carlos Bender ; Correia, Carlos Roque Duarte
Source: Tetrahedron. Unidade: IQSC
Subjects: PRODUTOS NATURAIS, QUÍMICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURTOLOSO, Antonio Carlos Bender e CORREIA, Carlos Roque Duarte. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, v. 64, n. 42, p. 9928-9936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.08.001. Acesso em: 03 nov. 2024.
APA
Burtoloso, A. C. B., & Correia, C. R. D. (2008). Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones. Tetrahedron, 64( 42), 9928-9936. doi:10.1016/j.tet.2008.08.001
NLM
Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001
Vancouver
Burtoloso ACB, Correia CRD. Stereoselective synthesis of azetidine-derived glutamate and aspartate analogues from chiral azetidin-3-ones [Internet]. Tetrahedron. 2008 ; 64( 42): 9928-9936.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2008.08.001
Artigo de periodico
Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles (2003)
Pérez, Eduardo R.; Loupy, André; Liagre, Marion; Plepis, Ana Maria de Guzzi ; Cordeiro, Paulo Jorge Marques
Source: Tetrahedron. Unidade: IQSC
Subjects: QUÍMICA, FUNGICIDAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PÉREZ, Eduardo R. et al. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles. Tetrahedron, v. 59, p. 865-870, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(02)01622-8. Acesso em: 03 nov. 2024.
APA
Pérez, E. R., Loupy, A., Liagre, M., Plepis, A. M. de G., & Cordeiro, P. J. M. (2003). Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles. Tetrahedron, 59, 865-870. doi:10.1016/s0040-4020(02)01622-8
NLM
Pérez ER, Loupy A, Liagre M, Plepis AM de G, Cordeiro PJM. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles [Internet]. Tetrahedron. 2003 ; 59 865-870.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(02)01622-8
Vancouver
Pérez ER, Loupy A, Liagre M, Plepis AM de G, Cordeiro PJM. Clean and efficient microwave-solvent-free synthesis of 1-(2',4'-dichlorophenacyl) azoles [Internet]. Tetrahedron. 2003 ; 59 865-870.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(02)01622-8
Artigo de periodico
An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene (2002)
Alves, C. N.; Silva, Alberico Borges Ferreira da ; Martí, S.; Moliner, V.; Oliva, M.; Andrés, J.; Domingo, L. R.
Source: Tetrahedron. Unidade: IQSC
Assunto: QUÍMICA TEÓRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, C. N. et al. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene. Tetrahedron, v. 58, n. 13, p. 2695-2700, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(02)00072-8. Acesso em: 03 nov. 2024.
APA
Alves, C. N., Silva, A. B. F. da, Martí, S., Moliner, V., Oliva, M., Andrés, J., & Domingo, L. R. (2002). An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene. Tetrahedron, 58( 13), 2695-2700. doi:10.1016/s0040-4020(02)00072-8
NLM
Alves CN, Silva ABF da, Martí S, Moliner V, Oliva M, Andrés J, Domingo LR. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene [Internet]. Tetrahedron. 2002 ; 58( 13): 2695-2700.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(02)00072-8
Vancouver
Alves CN, Silva ABF da, Martí S, Moliner V, Oliva M, Andrés J, Domingo LR. An AM1 theoretical study on the effect of 'Zn POT.2+' Lewis acid catalysis on the mechanism of the cycloaddition between 3-phenyl-1-(2-pyridyl)-2-propen-1-one and cyclopentadiene [Internet]. Tetrahedron. 2002 ; 58( 13): 2695-2700.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(02)00072-8
Artigo de periodico
A study on the effect of Lewis acid catalysis on the molecular mechanism of the cycloaddition between (E)-methyl cinnamate and cyclopentadiene (2001)
Alves, C. N.; Camilo, F F; Gruber, Jonas ; Silva, Alberico Borges Ferreira da
Source: Tetrahedron. Unidades: IQ, IQSC
Assunto: QUÍMICA TEÓRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVES, C. N. et al. A study on the effect of Lewis acid catalysis on the molecular mechanism of the cycloaddition between (E)-methyl cinnamate and cyclopentadiene. Tetrahedron, v. 57, p. 6877-6883, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0040-4020(01)00624-x. Acesso em: 03 nov. 2024.
APA
Alves, C. N., Camilo, F. F., Gruber, J., & Silva, A. B. F. da. (2001). A study on the effect of Lewis acid catalysis on the molecular mechanism of the cycloaddition between (E)-methyl cinnamate and cyclopentadiene. Tetrahedron, 57, 6877-6883. doi:10.1016/s0040-4020(01)00624-x
NLM
Alves CN, Camilo FF, Gruber J, Silva ABF da. A study on the effect of Lewis acid catalysis on the molecular mechanism of the cycloaddition between (E)-methyl cinnamate and cyclopentadiene [Internet]. Tetrahedron. 2001 ; 57 6877-6883.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(01)00624-x
Vancouver
Alves CN, Camilo FF, Gruber J, Silva ABF da. A study on the effect of Lewis acid catalysis on the molecular mechanism of the cycloaddition between (E)-methyl cinnamate and cyclopentadiene [Internet]. Tetrahedron. 2001 ; 57 6877-6883.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/s0040-4020(01)00624-x

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Non normalized affiliation